DeLay Bridget D, Krneta-Stankic Vanja, Miller Rachel K
Department of Pediatrics, Pediatric Research Center, University of Texas McGovern Medical School.
Department of Pediatrics, Pediatric Research Center, University of Texas McGovern Medical School; Program in Genes & Development, University of Texas Graduate School of Biomedical Sciences.
J Vis Exp. 2016 May 3(111):53799. doi: 10.3791/53799.
The embryonic kidney of Xenopus laevis (frog), the pronephros, consists of a single nephron, and can be used as a model for kidney disease. Xenopus embryos are large, develop externally, and can be easily manipulated by microinjection or surgical procedures. In addition, fate maps have been established for early Xenopus embryos. Targeted microinjection into the individual blastomere that will eventually give rise to an organ or tissue of interest can be used to selectively overexpress or knock down gene expression within this restricted region, decreasing secondary effects in the rest of the developing embryo. In this protocol, we describe how to utilize established Xenopus fate maps to target the developing Xenopus kidney (the pronephros), through microinjection into specific blastomere of 4- and 8-cell embryos. Injection of lineage tracers allows verification of the specific targeting of the injection. After embryos have developed to stage 38 - 40, whole-mount immunostaining is used to visualize pronephric development, and the contribution by targeted cells to the pronephros can be assessed. The same technique can be adapted to target other tissue types in addition to the pronephros.
非洲爪蟾(青蛙)的胚胎肾,即前肾,由单个肾单位组成,可作为肾脏疾病的模型。非洲爪蟾胚胎体积大,在体外发育,并且可以通过显微注射或外科手术轻松操作。此外,已经建立了早期非洲爪蟾胚胎的命运图谱。对最终将发育为感兴趣器官或组织的单个卵裂球进行靶向显微注射,可用于在该受限区域内选择性地过表达或敲低基因表达,减少发育中胚胎其他部分的次要影响。在本方案中,我们描述了如何利用已建立的非洲爪蟾命运图谱,通过对4细胞和8细胞胚胎的特定卵裂球进行显微注射,来靶向发育中的非洲爪蟾肾脏(前肾)。注射谱系示踪剂可验证注射的特异性靶向。胚胎发育到38 - 40期后,采用整体免疫染色来观察前肾发育情况,并评估靶向细胞对前肾的贡献。除了前肾之外,相同的技术还可用于靶向其他组织类型。